Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:39390860-39390914 | Rare:25 | ||||
chr19:39391025-39391425 | Common:1; Rare:161 | ||||
chr19:39406684-39406938 | Rare:97 | ||||
chr19:39407208-39407446 | Rare:38 | ||||
chr19:39413647-39413820 | Rare:33 | ||||
chr19:39480716-39480912 | Common:3; Rare:106; Clinvar (pathogenic):1 | ||||
chr19:39846308-39846539 | Common:1; Rare:112 | ||||
chr19:39970933-39971214 | Common:4; Rare:79 | ||||
chr19:39996956-39997074 | Common:4; Rare:37 | ||||
chr19:40056157-40056288 | Rare:18 | ||||
chr19:40090865-40091006 | Common:1; Rare:38 | ||||
chr19:40348388-40348739 | Common:4; Rare:117 | ||||
chr19:40465680-40466043 | Common:2; Rare:117 | ||||
chr19:40601218-40601388 | Rare:54 | ||||
chr19:40601545-40601589 | Rare:9 |